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Search / Trial NCT05460416

Treatment Preventive for Pre-eclampsia by Acetylsalicylic Acid in Women Who Underwent Frozen Embryo Transfer

Launched by CENTRE HOSPITALIER UNIVERSITAIRE DE LIEGE · Jul 13, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Embryo Transfer Hypertension, Pregnancy Induced

ClinConnect Summary

This clinical trial is studying whether taking a low dose of acetylsalicylic acid (commonly known as aspirin) can help prevent pre-eclampsia in pregnant women who have undergone frozen embryo transfer. Pre-eclampsia is a condition that can occur during pregnancy, causing high blood pressure and other health issues. The trial is currently looking for healthy women aged 18 to 43 who are planning to have a frozen embryo transfer and have confirmed their pregnancy by six weeks.

To participate, women must not have certain risk factors for pre-eclampsia, such as a history of the condition, being significantly overweight, or having other health issues like untreated high blood pressure or diabetes. Participants in the trial will take the low-dose acetylsalicylic acid and will be monitored to see if it helps reduce the chances of developing pre-eclampsia. It's essential for potential participants to understand the inclusion and exclusion criteria to determine if they are eligible for this important research study.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Healthy women from \[18 - 43\] years-old, planned for a frozen embryo transfer, with natural and modified natural or HRT cycle
  • Who have given their informed consent
  • Who have a confirmed pregnancy at week 6 of amenorrhea.
  • Exclusion Criteria:
  • Women presenting one risk factor for preeclampsia: multiple pregnancy, history of preeclampsia, BMI \> 30, lupus syndrome, preexistent proteinuria, non-treated chronic high blood pressure (\>140/90), antiphospholipid antibody syndrome, diabetes (fasting blood sugar \>126mg/dl)
  • Contraindication to acetylsalicylic acid (at risk of active hemorrhage (like hemophilia, ...); at risk of or who have a gastro-duodenal ulcer; at risk or how have a terminal renal or hepatic in-sufficiency (only if acetylsalicylic acid is given at high dose)
  • Already treated with acetylsalicylic acid
  • Treatment with anticoagulants or non-steroid anti-inflammatory drugs

About Centre Hospitalier Universitaire De Liege

The Centre Hospitalier Universitaire de Liège (CHU Liège) is a leading academic medical center in Belgium, renowned for its commitment to advancing healthcare through innovative clinical research and comprehensive patient care. As a prominent sponsor of clinical trials, CHU Liège integrates cutting-edge scientific inquiry with clinical practice, fostering an environment that enhances the development of new therapies and medical interventions. With a multidisciplinary team of experienced researchers and healthcare professionals, the institution is dedicated to improving patient outcomes and contributing to the global body of medical knowledge. CHU Liège emphasizes collaboration with industry partners and academic institutions to drive excellence in clinical research and support the translation of findings into real-world applications.

Locations

Liège, , Belgium

Liège, , Belgium

Patients applied

0 patients applied

Trial Officials

Laurie Henry

Principal Investigator

Centre Hospitalier Régional de la Citadelle

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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